Co(III) or Ru(II)-Catalyzed Selective C–H Alkynylation of 2-Pyridones and Their Derivatives with Bromoalkynes DOI

Quanjian Luo,

Han‐Chi Wang,

Jierui Zhou

и другие.

The Journal of Organic Chemistry, Год журнала: 2024, Номер unknown

Опубликована: Дек. 5, 2024

We successfully reported selective C–H alkynylation of 2-pyridones with bromoalkynes under the catalysis Co(III) or Ru(II). The reaction used easily accessible instead high-valent iodine alkynes. There is a broad substrate scope good yields. In addition, 2-pyridone can be as weakly directing group for proximal aryl bond. This method offers an efficient approach synthesizing diverse derivatives, yielding alkynylated products up to 95% yield (>40 examples).

Язык: Английский

Ru(II)‐Catalyzed Selective C—H Alkynylation of Isoquinolones, Quinazolones and Phthalazinones with Bromoalkynes DOI

Quanjian Luo,

Han‐Chi Wang,

Jing Zhang

и другие.

Chinese Journal of Chemistry, Год журнала: 2024, Номер 42(15), С. 1686 - 1690

Опубликована: Март 15, 2024

Comprehensive Summary A new, selective Ru(II)‐catalyzed alkynylation reaction of isoquinolones, quinazolones and phthalazinones with readily available bromoalkynes has been developed. This enables the construction a new C(sp 2 )‐C(sp) bond through C—H activation C—Br functionalization, offers an effective route to synthesizing highly valuable alkynylated isoquinolone, quinazolone phthalazinone derivatives wide substrate scope high selectivity.

Язык: Английский

Процитировано

3

Ru(II)-Catalyzed C–H Amination of 1,2,3-Benzotriazinones with Azide Compounds DOI

Han‐Chi Wang,

Quanjian Luo,

Jin‐Heng Li

и другие.

The Journal of Organic Chemistry, Год журнала: 2024, Номер 89(17), С. 12249 - 12254

Опубликована: Авг. 8, 2024

A Ru(II)-catalyzed directed C–H amination of 1,2,3-benzotriazinones with azide compounds has been reported. The reaction a wide substrate scope organic azides good results and represents useful pathway to the construction versatile heterocyclic amino products. In addition, method can be used for phthalazinones, highlighting synthetic practicability strategy.

Язык: Английский

Процитировано

2

Recent approaches for the synthesis of heterocycles from amidines via metal catalyzed C-H functionalization reaction DOI
Youpeng Zuo,

Pengfei Zuo,

Meijun Liu

и другие.

Organic & Biomolecular Chemistry, Год журнала: 2024, Номер 22(25), С. 5014 - 5031

Опубликована: Янв. 1, 2024

Transition metal catalyzed C-H bond activation has become one of the most important tools for constructing new chemical bonds. Introducing directing groups to substrates is key a successful reaction, these can also be further transformed in reaction. Amidines with their unique structure and reactivity are ideal transition metal-catalyzed transformations. This review describes major advances mechanistic investigations activation/annulation tandem reactions amidines until early 2024, focusing on unsaturated compounds, such as alkynes, ketone, vinylene carbonate, cyclopropanols derivatives. Meanwhile this manuscript explores reaction different carbene precursors, example diazo azide, triazoles, pyriodotriazoles, sulfoxonium ylides well own activation/cyclization reactions. A bright outlook provided at end manuscript.

Язык: Английский

Процитировано

0

Co(III) or Ru(II)-Catalyzed Selective C–H Alkynylation of 2-Pyridones and Their Derivatives with Bromoalkynes DOI

Quanjian Luo,

Han‐Chi Wang,

Jierui Zhou

и другие.

The Journal of Organic Chemistry, Год журнала: 2024, Номер unknown

Опубликована: Дек. 5, 2024

We successfully reported selective C–H alkynylation of 2-pyridones with bromoalkynes under the catalysis Co(III) or Ru(II). The reaction used easily accessible instead high-valent iodine alkynes. There is a broad substrate scope good yields. In addition, 2-pyridone can be as weakly directing group for proximal aryl bond. This method offers an efficient approach synthesizing diverse derivatives, yielding alkynylated products up to 95% yield (>40 examples).

Язык: Английский

Процитировано

0